JPRN-jRCTb050220148招募中1 期
An open-label study on the efficacy and safety of subcutaneous adipose tissue-derived cell aggregates (S-ADSCs) transplantation using an adhesive cell culture plate for knee osteoarthritis - OL-ES-S-ADSCs-KOA
Sobajima Satoshi0 个研究点目标入组 10 人开始时间: 2023年1月5日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 ot applicable(—)
- 性别
- All
入选标准
- •Patients with dysfunction associated with osteoarthritis
- •-Over 20 years old when obtaining consent
- •-Diagnosed with osteoarthritis of the knee at our hospital, and there is no improvement even after implementing standard conservative therapy (hyaluronic acid injection and physical therapy) that is fully covered by insurance for more than 3 months.
- •-After standard conservative therapy for 3 months or more, pain evaluation value of 40 or more by visual analogue scale
- •-Don't wish to perform artificial joint replacement or osteotomy
- •-Obtain written consent sufficient explanation about this study
- •-Able to comply with a fixed schedule
排除标准
- •-Patients who have difficulty in subcutaneous liposuction
- •-Patients with cancer
- •-Pregnant women, lactating women and patients who may become pregnant
- •-Patients using anticancer drugs, biopharmacy or immunosuppressive drugs
- •-Patients with active infection
- •-Patients who have received intra-articular transplantation of S-ADSCs in the past
- •-Patients who have received this treatment within 1 month
- •-Patients with serious complications (heart disease, lung disease, liver disease, renal disease, bleeding tendency, uncontrolled diabetes and hypertension, etc.) that the doctor deems inappropriate
- •-Patients with a history of drug hypersensitivity to anesthetics, etc.
- •-Other patients who the attending physician deems inappropriate
研究者
相似试验
进行中(未招募)
1 期
Evaluation of Zepatier in a community-based setting among hepatitis infected cirrhotic and non-cirrhotic patients on stable opiate substitution therapy.HCV Genotypes 1/4EUCTR2016-003414-26-IEDr. John Lambert (Mater Misericordiae University Hospital)60
未知
3 期
Open-label study to assess efficacy and safety of a single dose (i.v.) of NMA78 in PS or ET patients and HVPS:Parkinson's Disease (PD), Multiple System Atrophy (MSA), Progressive Supranuclear Palsy(PSP), ETJPRN-jRCT2080221472ihon Medi-Physics Co., Ltd.24
未知
3 期
Open-label study to assess efficacy and safety of a single dose (i.v.) of NMA78 in DLB or AD patients and HVDLB, ADJPRN-jRCT2080221473ihon Medi-Physics Co., Ltd.18
已完成
3 期
A study assessing safety and efficacy of MD-16 intraocular lens in patients with aphakic eye after cataract surgeryCataractJPRN-jRCT1080223821SANTEN PHARMACEUTICAL Co., LTD.59
进行中(未招募)
1 期
Safety and Efficacy study assessing PRX 102 in Patients with Fabry Disease currently treated with REPLAGAL® (Agalsidase alfa)Fabry disease (a-galactosidase A deficiency)MedDRA version: 20.0Level: PTClassification code 10016016Term: Fabry's diseaseSystem Organ Class: 10010331 - Congenital, familial and genetic disordersEUCTR2016-001318-11-DEProtalix Ltd.22
